Location analysis using nucleic acid-labeled tags

ABSTRACT

A method for using information encrypted with a nucleic acid molecule to backtrack an item&#39;s path or identify a point of origin. Unique nucleic acid-containing tags are seeded at one or more geographic locations. Using sequence analysis techniques, the person or object of interest is examined for the presence of one or more of the seeded nucleic acids. The geographic location associated with each detected nucleic acid is used to backtrack the item&#39;s path or extrapolate a probable point of origin.

BACKGROUND OF THE INVENTION

1. Field of the Invention

The present invention relates to a method for using nucleic acid-labeledtags, and, more particularly, using nucleic acid-labeled tags forlocation analysis.

2. Description of the Related Art

The physical characteristics of a nucleic acid molecule make it uniquelysuitable for use as a secure information-storage unit. In addition tobeing odorless and invisible to the naked eye, a nucleic acid moleculecan store vast amounts of information. It has been estimated that asingle gram of deoxyribonucleic acid (“DNA”) can store as muchinformation as approximately one trillion compact discs (“Computing WithDNA” by L. M. Adleman, Scientific American, August 1998, pg 34-41).

Nucleic acid molecules are also resilient to decay, even in vitro.Although a nucleic acid molecule typically begins to breakdown whenexposed to chemicals, radiation, or enzymes, some nucleic acid moleculescan survive for thousands of years. For example, scientists havesequenced the Neanderthal genome using DNA molecules that were recoveredfrom remains dating at least 38,000 years old.

Lastly, nucleic acid molecules are both ubiquitous in nature and largelyuncharacterized, with only a fraction of the world's organisms havingbeen sequenced. As a result of this uncharacterized environmentalbackground noise, inadvertent detection of a man-made nucleic acidmolecule is unlikely.

To employ the many beneficial characteristics of nucleic acids, thesemolecules can be incorporated into a secure tag. These tags can becomposed of deoxyribonucleotides, ribonucleotides, or similar moleculescomposed of nucleic acids that are either artificial (such as nucleotideanalogues) or are otherwise found in nature. The nucleic acids can rangefrom very short oligonucleotides to complete genomes.

Once a nucleic acid tag is created it can be used for numerous uniquesecurity applications including to: (i) detect illicit tampering withphysical objects; (ii) secure the privacy of a room or building; (iii)send encoded messages between individuals; (iv) detect a taggedindividual or object at a distance; (v) track the recent travel historyof an individual or object; or (vi) monitor a location of interest.

DNA tags have previously been used for other applications. For example,DNA tags have been removably attached to tangible assets to assist inthe identification of ownership in the event the asset is lost orstolen. Additionally, it has been proposed that DNA tags be used toprevent counterfeiting by incorporating tags into items during or afterproduction and using detection of such tags to authenticate the items.

SUMMARY OF THE INVENTION

It is therefore a principal object and advantage of the presentinvention to provide a nucleic acid tag that can be used in numeroussecurity-related applications.

It is a further object and advantage of the present invention to providea method of standoff detection using nucleic acid tags.

It is yet another object and advantage of the present invention toprovide a method of determining whether an object has traveled through alocation using seeded nucleic acid-labeled tags.

It is a further object and advantage of the present invention tobacktrack or identify an object's point of origin or recent geographiccourse using seeded nucleic acid-labeled tags.

Other objects and advantages of the present invention will in part beobvious, and in part appear hereinafter.

In accordance with the foregoing objects and advantages, the presentinvention provides a method of determine whether an item has movedthrough a geographic location, the method comprising: (a) creating anucleic acid tag containing a nucleic acid; (b) seeding the geographiclocation with the nucleic acid tag; and (c) examining the item for thepresence of the nucleic acid tag.

A further embodiment of the present invention is a method forbacktracking the travel history of an item, the method comprising: (a)creating two or more nucleic acid tags, said nucleic acid tags comprisedof a nucleotide-support platform attached to at least one nucleic acidmolecule; (b) seeding each of two or more geographic locations with saidnucleic acid tags, wherein each geographic location is seeded with aunique nucleic acid tag; (c) examining said item for the presence of oneor more nucleic acid tags; and (d) identifying the geographic locationassociated with each nucleic acid tag detected on the item.

Another embodiment of the present invention is a method for determiningthe point of origin of an item, the method comprising: (a) creating twoor more nucleic acid tags, said nucleic acid tags comprised of anucleotide-support platform attached to at least one nucleic acidmolecule; (b) seeding each of two or more geographic locations with saidnucleic acid tags, wherein each geographic location is seeded with aunique nucleic acid tag; (c) examining said item for the presence of oneor more nucleic acid tags; and (d) identifying the geographic locationassociated with each nucleic acid tag detected on the item; and (e)extrapolating the point of origin.

Yet another embodiment of the present invention is a method foridentifying the presence of a luminescent nucleic acid tag on an itemcomprising: (a) irradiating said item with photons of a firstwavelength; (b) scanning for emission of photons of a second wavelengthfrom said item; and (c) determining the presence of said luminescentnucleic acid tag on said item by detecting said photons of a secondwavelength.

BRIEF DESCRIPTION OF THE DRAWINGS

The present invention will be more fully understood and appreciated byreading the following Detailed Description of the Invention inconjunction with the accompanying drawings, in which:

FIG. 1 is a schematic representation of nucleic acid tag production.

FIG. 2 is a schematic representation of an embodiment of the methodaccording to the present invention.

FIG. 3 is a side view of an encapsulated nucleotide tag complex.

FIG. 4 is a side view of encapsulated nucleotide-derivatizednanoparticles.

FIG. 5 is a side view of an encapsulated tag complex containing aretroreflector and nucleotide-derivatized nanoparticles.

FIG. 6 is a side view of an encapsulated nucleotide tag complex withseparate marker elements.

FIG. 7 is a side view of an encapsulated nucleotide tag complex withmarker elements coating the outer surface of the encapsulant.

FIG. 8 is a side view of an encapsulated nucleotide tag complex withmarker elements incorporated into the encapsulant layer.

FIG. 9 is a side view of an encapsulated nucleotide tag complex withmarker elements incorporated into the nanoparticles.

FIG. 10 is a side view of an encapsulated nucleotide tag complex withmarker elements trapped inside the tag by the encapsulant layer.

DETAILED DESCRIPTION OF THE INVENTION

Referring now to the drawings wherein like reference numerals designateidentical or corresponding parts throughout the several views, there isshown in FIG. 1 a schematic representation of nucleic acid tagproduction. As an initial step 10, a nanometer-sized particle(“nanoparticle”) platform is prepared for attachment to the nucleic acidmolecule(s). A platform is used to make the nucleic acid more accessibleto downstream analysis and prevent nucleic acid loss if any portion ofthe encapsulating layer is compromised.

The platform is any compound that can be attached to nucleic acidwithout unintentionally degrading or altering the nucleic acid sequence.For example, the platform can be a lightweight, durable, non-watersoluble, and chemically inert structure composed of silica orpolystyrene. Additionally, the nanoparticle platform should be composedof a compound that does not inhibit any downstream analysis of thenucleic acid molecules, including tag detection and polymerase chainreaction (“PCR”).

In step 12, the nucleic acid molecule is attached to the preparednanoparticle platform. The nucleic acid molecules are optimally attachedto the nanoparticle to facilitate later analysis. In a preferredembodiment, a chemical linker is used to connect the nucleic acid to thenanoparticle platform. This chemical linker must keep the nucleic acidsecurely tethered to the nanoparticle while avoiding inhibition of thedetection or analysis of the tag and nucleic acid. Although the chemicallinker can be chosen to provide a permanent covalent link between thenucleic acid and the nanoparticle platform, it could also be a compoundthat quickly and efficiently releases the nucleic acid at a certaintemperature or after exposure to a release compound.

The nucleic acid molecule can also be designed to promote analysis. Forexample, to avoid steric hindrance or unwanted intermolecularinteractions, the molecule can include nucleotide spacers between thechemical linker or nanoparticle base and the information-coding segmentof the nucleotide sequence. Spacing between 5 and 15 bases has beenoptimal for current applications, although this may vary as newapplications are considered.

The concentration of nucleic acid molecules on the nanoparticle platformis also an important factor in downstream analysis. If the molecules aretoo concentrated, steric hindrance prevents the primer and polymerasefrom efficiently binding the proper segments of the nucleic acidmolecules. If the molecules are too sparse, the PCR signal will bediminished and can result in false negatives. In the preferredembodiment, a concentration of about 3×10¹⁰ nucleic acid molecules persquare centimeter is the optimal concentration for robust PCR signal.

In step 14, the nucleic acid-derivatized nanoparticles are agglomerated.Agglomeration protects the nucleic acid molecules from degradation andfacilitates encapsulation. To agglomerate the particles to the desiredsize range, the nanoparticles are vacuum dried, milled, and sieved.

Compounds might be used or incorporated into the tag to promotedisagglomeration of the agglomerates prior to PCR analysis. Thesecompounds might be bovine serum albumin, salmon sperm DNA,carbohydrates, polyvinyl alcohol, fructose, or chitosan, among others.With more nucleic acid exposed during dissolution, subsequent analysiswill be faster and more sensitive.

After the nanoparticles are agglomerated, the agglomerates areencapsulated in step 16. The encapsulant protects the nucleic acid fromdegradation by ultraviolet light, hydrolysis, enzymatic digestions,chemical degradation, or any other means. Additionally, the encapsulantcan be designed such that it does not hinder analysis of the nucleicacid molecules. For example, the encapsulant should not contain anycompounds that would inhibit or prevent a PCR reaction, althoughefficient removal of the encapsulant before PCR analysis would eliminatethis requirement. Additionally, the encapsulant should enhance theability of the tag to discretely attach to people and objects. Ifcovertness is required, the encapsulant can be designed to deterdetection.

The encapsulating layer can also be designed with surface moieties addedto the inner or outer surfaces of the encapsulant or incorporated intothe encapsulant material. The moieties are designed to facilitate aparticular use of the nucleic acid tag. For example, the moiety can behydrophobic to enable stickiness or contain antibodies designed forspecific targeting. The molecular interactions between the moiety and atarget compound can range from simple electrostatic interactions toantibody-antigen recognition. The moiety can also promote detection ofthe nucleic acid tag.

To protect the nucleic acid from degradation, the encapsulating layercan be coated with or include another functional layer of material. Forexample, the encapsulant can be coated with or include anon-water-soluble compound to prevent access to water or similarmolecules. The encapsulant can also be coated with or include aUV-blocking compound such as titanium dioxide to prevent UV-induceddegradation of the nucleic acid molecules.

FIG. 2 is a schematic representation of an embodiment of a securitymethod according to the present invention. More specifically, the figurerepresents characterization of the recent travel history of point of anitem. An item can be any person or object of interest. Seeding an areawith tags that naturally or artificially adhere to objects (includingpeople or animals) provides a mechanism for identifying the origin ofthose objects simply by analyzing the adhering tags. Similarly, byseeding different areas with discernibly different tags it is possibleto backtrack the geographic path that an object has followed. Such amechanism would allow the seeder—the person or organization who seededand will analyze the tags—to identify the recent travel history of theperson or object; to quickly identify people or objects that havetraveled through seeded areas; and to identify vehicles that havetraveled through seeded areas and might carry dangerous cargo such asexplosives, among other uses.

As an initial step 18, an identifiable nucleic acid is characterized orcreated. In one embodiment of the present invention, the sequence rangesfrom a short oligonucleotide to an entire genome and is generatedthrough any of the various known methods of natural or artificialnucleic acid synthesis. The nucleic acid can be completely composed ofeither natural nucleic acids which normally compose the genomes oforganisms, artificial nucleic acids, or a mixture of the two.

In the preferred embodiment of the tag, the nucleic acid molecules ofeach type of tag—which typically differ depending on location or mannerof use—contain identical primer—binding sequences surrounding uniquenucleotide sequences. Each unique nucleotide sequence contained betweenthe primers encodes information that corresponds to the location, time,or other data specific to that unique sequence. Since analysis of adetected tag uses the same primers, the analysis is performed faster andmore efficiently.

The primer sequences, whether they are unique or identical for eachlocation or use, are chosen to avoid cross-reactions withnaturally-occurring nucleic acid molecules in the environment in whichthe tag is located. Although only a fraction of natural nucleic acidmolecules on Earth have been characterized by scientists, the search ofnucleic acid repository databases such as GenBank®, the NationalInstitutes of Health database containing all publicly available DNAsequences, should be a preliminary step in constructing the primersequences.

In one embodiment of the current invention, unique groupings ofnucleotides are assigned a specific letter, number, or symbol value inorder to encode information within the sequence. By placing the uniquegroupings in order, information can be encrypted into the nucleotidesequence. To further increase the security of the information, advancedencryption algorithms can be used to assign letter, number, or symbolvalues to specific nucleotides or nucleotide groupings. Additionally,the encryption system can be periodically changed to prevent decryptionby intercepting entities.

The nucleic acid can also be encoded to contain information other than astring of letters, numbers, and symbols. For instance, the sequence canbe a random sequence that corresponds to the latitude and longitude ofthe site that will be seeded. Alternatively, the tag can be as simple asa single nucleic acid change in a previously identified or knownsequence. For example, the nucleotide sequence can be embedded in a fullor partial genomic sequence corresponding to an organism which naturallyexists in the location to be seeded. Modifications to the naturalnucleic acid sequence, known only to the creator of the tag, can be madesuch that the changes resemble natural variations of the sequence andthus fail to arouse suspicion, even by individuals that might suspectsuch tags are present.

To decrypt the encoded information according to this system, anindividual will need: (1) knowledge that encoded nucleic acid ispresent; (2) knowledge of the specific location of the informationwithin the nucleic acid in order to use the appropriate primers foramplification and sequencing reactions; (3) access to a PCR machine andreagents; and (4) the encryption algorithm, or, alternatively, complexdecryption capabilities.

Although creating the tag within the genome of an naturally-occurringorganism provides numerous benefits, both in vivo and in vitro DNAreplication occasionally introduces random errors into a DNA sequencedespite the actions of proof-reading and repair enzymes. By deleting oneor more nucleotides or frame-shifting the nucleic acid sequence, thesemutations can disrupt any encrypted information contained therein.Computer algorithms are used to restore the information by recognizingand repairing the errors. For example, if a mutation adds one or morenucleotides to a pre-defined sequence and disrupts the information, thealgorithm removes single or multiple nucleotides from the sequence untilthe information is corrected. Similarly, if a mutation removes one ormore nucleotides, the algorithm systematically adds nucleotides to thesequence until the information is corrected. The algorithm must also berobust enough to decrypt sequences that contain more than one type oferror-inducing mutation, and must be capable of recognizing when theinformation contained with the nucleic acid has been restored.

In step 20 of FIG. 1, the nucleic acid is packaged into an appropriatetag complex. To avoid potentially harmful environmental side-effects,the tag can be large enough to avoid being inhaled by people ororganisms but small enough to be covert. FIG. 3 represents oneembodiment of this tag structure. Tag 30 is composed of a singlenucleotide-support platform 32, nucleic acid 34, and encapsulant 36.

FIG. 4 is a side view of another embodiment of the tag structure. Tag 38is composed of nucleotide-support platform 40 derivatized with nucleicacid 42 and surrounded by encapsulant 44. Similar to the tag in FIG. 3,tag 38 contains nucleic acids that are contained within an encapsulantthat protects the sequence without inhibiting later analysis. Unlike thebead platform used by the tag in FIG. 3, nucleotide-support platform 40is composed of nanoparticles. Tag 38 can contain thousands, millions, oreven billions of nucleotide-derivatized nanoparticles within theencapsulant layer.

FIG. 5 is yet another embodiment of the tag complex. Encapsulated tag 46contains a retroreflector 48, nucleotide-derivatized nanoparticles 50,and encapsulant 52. Retroflector 48, a device that reflects anelectromagnetic wave front back along a vector that is parallel to butopposite in direction from the angle of incidence, forms the center oftag 46. The retroreflector must be situated to allow electromagneticwaves to hit and reflect from the surface. To prevent obstruction of theretroreflector, the tag is organized to keep nucleotide-derivatizednanoparticles 50 away from the surface of the retroreflector, as shownin FIG. 5. Additionally, encapsulant 52 must protect the tag complexwithout interfering with the retroreflector's reflectivity. As analternative to the nanoparticle format shown in FIG. 5, the nucleic acidcan coat the non-reflective surfaces of retroreflector 48. In anotherembodiment of the retroreflector tag, the non-reflective surfaces of theretroreflector are coated with nucleic acid and only those surfaces arecovered by a protective encapsulant.

In step 22 of FIG. 2, one or more geographic locations are seeded withthe tags. The locations are seeded with tags using any mechanism thatwill adequately disperse the tags at the desired concentration. Forexample, the tags can be seeded on and along roadways or paths using anautomobile that has been modified to disperse the tags. The tags canalso be discretely dispersed from the air using an airplane orremotely-controlled flying apparatus. Tags can even be seeded byindividuals using hand-held dispersal systems.

To efficiently backtrack the movements of a person, vehicle, or object,each road within a given location can be seeded with a unique tag. Asthe vehicle moves through the location it picks up tags from each roadit traverses. This system can be scaled up or scaled down to suit theneeds of the seeder. For example, rather than seeding individual roadsthe seeder can use the tags to label large regions of land to backtracklarge-scale movements. Alternatively, the seeder can scale down themethod by seeding individual homes or buildings to identify individualsor objects that have entered those buildings.

In step 24 of FIG. 2, an item is examined for the presence of seededtags. Once an object of interest is identified, the object can beexamined for seeded tags using any mechanism designed to pick up tagsfrom the surfaces of the object. For example, the tires, wheel wells, orunderside of a vehicle can be swabbed for tags. If the object ofinterest is a person, the individual's clothes, shoes, hair, or skin canbe swabbed for tags. If the object of interest is a post-blast fragmentof an explosive device, the surfaces of the fragment can be swabbed forany tags that survived the explosion.

If the seeded tags contain retroreflectors, electromagnetic waves can beused to detect the presence of tags. Scanning equipment shines light onthe object of interest and looks for a wave front that is reflectedalong a vector that is parallel to but opposite in direction from thewave's source. This suggests that retroreflective tags are present onthe surface of the object and alerts the authorities that furtherinvestigation is necessary. This rapid and cost-effective identificationof retroreflective tags is especially useful for high-throughputlocations such as checkpoints and border crossings. Once theretroreflective tags are detected, they can be removed from the surfacesof the object for analysis of the attached nucleic acids to identifygeographic locations.

The tags can also contain luminescent compounds that reveal theirpresence from a distance. Although the preferred embodiment usesfluorescent or phosphorescent photoluminescence, other embodiments mayinclude chemiluminesent, radioluminescent, or thermoluminescentcompounds. The photoluminescent compound is chosen such that absorptionof a photon with a certain wavelength by the compound causes theemission of a photon with a different wavelength. The difference betweenthe wavelength of the absorbed photon and the wavelength of the emittedphoton depends on the inherent physical properties of the chosencompound.

In the preferred embodiment, the luminescent compound absorbs and emitsphotons in the ultraviolet band—between 400 and 10 nanometers—of theelectromagnetic spectrum. The compound is chosen to avoid interferenceby UV radiation from the sun. The Earth's atmosphere absorbs as much as99% of the UV radiation emitted by the sun in the 150-320 nm range. Thusthe most advantageous luminescent compound absorbs and emits photonswith wavelengths below 320 nm.

As an alternative to luminescent compounds that absorb and emit photonsin the 150-320 nm range, compounds that absorb and emit photons ofwavelengths greater than 320 nm can be used under certain circumstances.For example, these compounds could be used during nighttime conditionsor in an enclosed UV-blocking environment such as a windowlessstructure.

The luminescent compound can be incorporated into the tag in a number ofdifferent ways. For example, in FIG. 6 the compound 54 is entirelyseparate from tag 38. In FIG. 7, compound 54 forms a layer on theexterior surface of encapsulant 44. The compound could also coat theinterior surface of encapsulant 44. In FIG. 8, compound 54 isincorporated into encapsulant 44. In FIG. 9, compound 54 coats thesurface of nucleotide-support platform 40. In FIG. 10, compound 54 isseparate from nucleotide-support platform 40 and encapsulant 44 but istrapped within the interior of tag 38. In several of the describedembodiments, the encapsulant layer must be designed to preventinhibition of excitation and emission wavelengths.

If the seeded tags contain a photoluminescent compound, electromagneticwaves can be used to detect the presence of tags at a distance. Scanningequipment shines photons of the excitatory wavelength on the object ofinterest and looks for photons emitted at the proper wavelength asdetermined by the compound used in the tags. Detection of photons withthe correct wavelength suggests that a nucleic acid-labeled tag ispresent and alerts the scanner that further investigation is necessary.The advantage of this system is that the scanning equipment and tag canbe designed such that the individual doing the scanning does not have tobe in close proximity to the object of interest.

The detection process can also be automated. An individual or object ofinterest can be forced to travel through a scanning point containingexcitation equipment and emission detection equipment. As the individualor object of interest travels through the scanning point, the equipmentscans for emitted photons of a certain wavelength. When the emittedphotons are detected, a computer at the scanning point automaticallyalerts a remotely-located entity that subsequent analysis is necessary.

In yet another embodiment of the current invention, the nucleic acidscontained within the tags taken from the surface of an object areanalyzed using any method that determines the exact order of nucleotidebases. There are currently a number of different commonly-usedsequencing techniques including but not limited to dye-terminatorsequencing, parallel sequencing, and sequencing by ligation. Sequencingmachines allow automated sequencing and can be run 24 hours a day. IfPCR techniques are used, the appropriate primers are chosen based uponthe types of tags known to be in the location of interest. Prior tosequencing or amplification, it is necessary to dissolve or otherwiseremove the encapsulant layer from the tag in a manner that avoidsinhibition of the downstream sequencing or PCR reactions. In thepreferred embodiment, the encapsulant and/or agglomerate is disrupted bybead beater, a form of mechanical disruption. This one-step methodavoids chemicals or extractions which could affect or inhibit PCRreactions.

In addition to the traditional sequencing techniques described above,real-time PCR and sequencing by hybridization techniques allow rapiddetection of target nucleic acids. According to the real-time PCRtechnique, the extracted nucleic acid is placed into a well or tube thathas been pre-loaded with all reagents necessary for a PCR reaction aswell as a sequence-specific, nucleotide-based, fluorescently-labeledprobe. As the extracted nucleic acid is amplified, the polymerasedegrades the probe and releases the fluorescent reporter. The reporterimmediately fluoresces and alerts the system to the presence of a tagnucleotide. Under the sequencing by hybridization technique, theextracted nucleic acid is labeled with a fluorescent marker and ishybridized to a DNA microarray that contains the complementarynucleotide sequence from known seeded tags. If the extracted nucleicacid hybridizes to any of the complementary tags, the fluorescent signalalerts the system to the presence of a target nucleic acid. Since bothmethods of analysis avoid additional analysis and require relativelyinexpensive analytical equipment, they promote faster and moreaffordable generation of data and require

In step 26 of FIG. 2, the sequences obtained from the identified tagsare compared to a database of sequences attached to seeded tags. Toefficiently determine the point of origin or recent travel history of anobject, the individuals analyzing tags detected in the field will needaccess or information about the tags dispersed by the seeder. A databaseof seeded tags will require maximum security measures to avoid improperaccess and manipulation, including access protection measures such aspasswords. Standard computer algorithms are used to find exact orapproximate matches between a sequence in the field and a tag sequencein the database. Once such a match is found, the user can reasonablysuspect that the object of interest has recently traveled through thelocation seeded by that tag. If the real-time PCR or sequencing byhybridization techniques are used, the identification of the seeded tagsis quickly determined by equipment that scans the plate or microarrayfor fluorescent label.

Step 28 of FIG. 2 is an optional step which is only required if the useris attempting to backtrack the route taken by an object of interest orextrapolate the object's point of origin. According to some uses of thepresent invention, simply learning that a person or object has traveledthrough a particular location is sufficient information. For other uses,it is necessary to analyze the sequences of multiple tags. Toextrapolate a route taken or a point of origin, the seeded tag locationinformation obtained by analyzing the surfaces of the object is fed intoa computer algorithm that quickly plots every potential route that theobject has traveled based upon the possible combinations of taglocations. A similar algorithm can be used to extrapolate a point oforigin based upon the identified tag locations.

Although the present invention has been described in connection with apreferred embodiment, it should be understood that modifications,alterations, and additions can be made to the invention withoutdeparting from the scope of the invention as defined by the claims.

1. A method for determining whether an item has moved through a geographic location, the method comprising: creating a nucleic acid tag comprised of a nucleotide-support platform attached to a nucleic acid molecule; seeding the geographic location with the nucleic acid tag; and examining the item for the presence of the nucleic acid tag.
 2. The method according to claim 1, wherein the nucleic acid molecule is composed of nucleotides selected from the group consisting of ribonucleotides, deoxyribonucleotides, and nucleotide analogues.
 3. The method according to claim 1, wherein the nucleic acid molecule is an oligonucleotide.
 4. The method according to claim 1, wherein the nucleic acid molecule is genomic deoxyribonucleic acid ranging from two nucleotides to the entire genome.
 5. The method according to claim 1, wherein information is encrypted within the nucleic acid molecule.
 6. The method according to claim 4, wherein information is encrypted within the genomic deoxyribonucleic acid molecule by altering the sequence of nucleotides.
 7. The method according to claim 1, wherein the nucleic acid tag is analyzed by sequencing all or part of the nucleic acid molecule.
 8. The method according to claim 1, wherein the nucleotide-support platform is a nanoparticle.
 9. The method according to claim 1, wherein the nucleic acid tag contains a retroreflector.
 10. The method according to claim 1, wherein the nucleic acid tag includes a luminescent compound.
 11. The method according to claim 10, wherein said luminescent compound emits photons with a wavelength within the range of ultraviolet radiation.
 12. The method according to claim 11, wherein said luminescent compound emits photons with a wavelength shorter than 320 nm.
 13. The method according to claim 1, wherein the presence of the nucleic acid tag is determined by exposing the item to electromagnetic radiation.
 14. The method according to claim 1, wherein the nucleic acid tag includes an encapsulant.
 15. The method according to claim 1, wherein each geographic location is seeded with a unique nucleic acid tag.
 16. A method for backtracking the travel history of an item, the method comprising: creating two or more nucleic acid tags, said nucleic acid tags comprised of a nucleotide-support platform attached to at least one nucleic acid molecule; seeding each of two or more geographic locations with said nucleic acid tags, wherein each geographic location is seeded with a unique nucleic acid; examining said item for the presence of one or more nucleic acid tags; and identifying the geographic location associated with each nucleic acid tag detected on said item.
 17. A method for determining the point of origin of an item according to claim 16, the method further comprising: extrapolating the point of origin.
 18. A method for identifying the presence of a luminescent nucleic acid tag on an item comprising: creatinq a luminescent nucleic acid tag comprising a luminescent compound, and further comprising a nucleotide-support platform attached to a nucleic acid molecule; seeding a geographic location with the luminescent nucleic acid tag; irradiating said item with photons of a first wavelength; scanning for emission of photons of a second wavelength from said item; and determining the presence of said seeded luminescent nucleic acid tag on said item by detecting said photons of a second wavelength.
 19. The method according to claim 18, further comprising: gathering said luminescent nucleic acid tag from said item.
 20. The method according to claim 19, further comprising: analyzing a nucleic acid molecule attached to said nucleic acid tag.
 21. The method according to claim 18, wherein said first wavelength and said second wavelength are within the range of ultraviolet radiation.
 22. The method according to claim 21, wherein said first wavelength and said second wavelength are shorter than 320 nm.
 23. A system for identifying the presence of a luminescent nucleic acid tag on an item, the system comprising: a luminescent nucleic acid tag comprising a luminescent compound, and further comprising a nucleotide-support platform attached to a nucleic acid molecule, wherein said luminescent nucleic acid tag is used to seed a geographic location; a radiation source, wherein the radiation source irradiates said item with photons of a first wavelength; a photon detection device in proximity to said item; a computer coupled to said photon detection device, wherein said computer includes processing means for alerting the system to the detection of a photon of a second wavelength. 